ADAMTS10 gene

Known as: ADAM metallopeptidase with thrombospondin type 1 motif 10, ADAMTS10, A DISINTEGRIN-LIKE AND METALLOPROTEINASE WITH THROMBOSPONDIN TYPE 1 MOTIF, 10 
 
National Institutes of Health

Papers overview

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2018
2018
The tumor suppressor protein RECK has been implicated in the regulation of matrix metalloproteinases (MMPs), NOTCH-signaling and… (More)
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2017
2017
We have previously described the expression and up-regulation of the C-terminal Binding Protein (CtBP) in response to pituitary… (More)
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Review
2015
Review
2015
Primary glaucomas are a leading cause of incurable vision loss in dogs. Based on their specific breed predilection, a genetic… (More)
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2014
2014
Primary glaucoma is one of the most common causes of irreversible blindness both in humans and in dogs. Glaucoma is an optic… (More)
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2011
2011
Autosomal recessive and autosomal dominant forms of Weill-Marchesani syndrome, an inherited connective tissue disorder, are… (More)
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2011
2011
Primary open angle glaucoma (POAG) is a leading cause of blindness worldwide, with elevated intraocular pressure as an important… (More)
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Highly Cited
2009
Highly Cited
2009
Weill-Marchesani syndrome (WMS) is a well-characterized disorder in which patients develop eye and skeletal abnormalities… (More)
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2008
2008
We report the identification and functional analysis of the first missense ADAMTS10 mutation (c.73G>A; p.Ala25Thr) causing… (More)
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2004
2004
We describe the discovery and characterization of ADAMTS10, a novel metalloprotease encoded by a locus on human chromosome 19 and… (More)
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Highly Cited
2004
Highly Cited
2004
Weill-Marchesani syndrome (WMS) is characterized by the association of short stature; brachydactyly; joint stiffness; eye… (More)
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